ANDEXXA (coagulation factor Xa (recombinant), inactivated-zhzo). Lyophilized powder for solution for intravenous injection. Initial U.S. Approval: 2018

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ANDEXXA (coagulation factor Xa (recombinant), inactivated-zhzo). Lyophilized powder for solution for intravenous injection. Initial U.S. Approval: 2018

ANDEXXA, coagulation factor Xa (recombinant), inactivated-zhzo is a recombinant modified human Factor Xa (FXa) protein indicated for patients treated with rivaroxaban or apixaban, when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding.
This indication is approved under accelerated approval based on the change from baseline in anti-FXa activity in healthy volunteers. An improvement in hemostasis has not been established. Continued approval for this indication may be contingent upon the results of studies to demonstrate an improvement in hemostasis in patients.
ANDEXXA is available as a lyophilized powder in single-use vials of 200 mg or 100 mg of coagulation factor Xa (recombinant), inactivated-zhzo.
Manufactured By: Portola Pharmaceuticals, Inc.
Prescribing Information URL: Click Here

Access to ANDEXXA ® (coagulation factor Xa (recombinant), inactivated-zhzo): Anticancer drugs available upon request. To get best price please share your mobile number to receive quotes from Medvitaz Pharma Solutions.

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FDA approved Anti-Cancer medicine ANDEXXA (coagulation factor Xa (recombinant), inactivated-zhzo) is available upon request. Get best retail price of ANDEXXA (coagulation factor Xa (recombinant), inactivated-zhzo) from trusted online pharmacy. For emergency product orders call 8750295029 (Mr. Neeraj Nagpal) or For enquires email For advanced treatments in India, Medvitaz Pharma Solution can even help patient to discuss with Occupational therapists .

Factor X is part of fresh frozen plasma and the prothrombinase complex. There are two commercially available Factor X concentrates: "Factor X P Behring" manufactured by CSL Behring, and high purity Factor X Coagadex produced by Bio Products Laboratory and approved for use in the United States by the FDA in October 2015, and in the EU in March 2016, after earlier acceptance by CHMP and COMP.


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